Denizci A A, Kazan D, Abeln E C A, Erarslan A
Research Institute for Genetic Engineering and Biotechnology, Marmara Research Center Campus, The Scientific and Technical Research Council of Turkey, Gebze, Kocaeli, Turkey.
J Appl Microbiol. 2004;96(2):320-7. doi: 10.1046/j.1365-2672.2003.02153.x.
The isolation and identification of new Bacillus sp. capable of growing under highly alkaline conditions as alkaline protease producers.
A Bacillus strain capable of growing under highly alkaline conditions was isolated from compost. The strain is a Gram-positive, spore-forming, motile, aerobic, catalase- and oxidase-positive, alkaliphilic bacterium and designated as GMBAE 42. Good growth of the strain was observed at pH 10. The strain was identified as Bacillus clausii according to the physiological properties, cellular fatty acid composition, G + C content of genomic DNA and 16S rRNA gene sequence analyses. The result of 16S rRNA sequence analyses placed this bacterium in a cluster with B. clausii. The G + C content of the genomic DNA of the isolate GMBAE 42 was found to be 49 mol%. The crude extracellular alkaline protease produced by the isolate showed maximal activity at pH 11.0 and 60 degrees C.
The results suggest that isolated strain GMBAE 42 is a new type of B. clausii capable of growing at pH 10.0 and produce extracellular alkaline protease very active at pH 11.0.
Isolated strain could be used in commercial alkaline protease production and its enzyme can be considered as a candidate as an additive for commercial detergents.
分离并鉴定能够在高碱性条件下生长的新型芽孢杆菌属菌株,作为碱性蛋白酶的产生菌。
从堆肥中分离出一株能够在高碱性条件下生长的芽孢杆菌菌株。该菌株为革兰氏阳性、产芽孢、具运动性、需氧、过氧化氢酶和氧化酶阳性的嗜碱细菌,命名为GMBAE 42。在pH 10时观察到该菌株生长良好。根据生理特性、细胞脂肪酸组成、基因组DNA的G + C含量以及16S rRNA基因序列分析,该菌株被鉴定为克劳氏芽孢杆菌。16S rRNA序列分析结果将该细菌与克劳氏芽孢杆菌归为一个簇。分离株GMBAE 42基因组DNA的G + C含量为49 mol%。该分离株产生的粗细胞外碱性蛋白酶在pH 11.0和60℃时表现出最大活性。
结果表明,分离株GMBAE 42是一种新型的克劳氏芽孢杆菌,能够在pH 10.0下生长,并产生在pH 11.0时具有高活性的细胞外碱性蛋白酶。
分离株可用于商业碱性蛋白酶的生产,其酶可被视为商业洗涤剂添加剂的候选物。